US2368690A - Process for the improvement of the properties of artificial masses and fibers manufactured from proteinlike substances - Google Patents
Process for the improvement of the properties of artificial masses and fibers manufactured from proteinlike substances Download PDFInfo
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- US2368690A US2368690A US303128A US30312839A US2368690A US 2368690 A US2368690 A US 2368690A US 303128 A US303128 A US 303128A US 30312839 A US30312839 A US 30312839A US 2368690 A US2368690 A US 2368690A
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- United States
- Prior art keywords
- fibers
- lanital
- chrome
- chromium
- treated
- Prior art date
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- Expired - Lifetime
Links
- 239000000835 fiber Substances 0.000 title description 28
- 238000000034 method Methods 0.000 title description 15
- 230000008569 process Effects 0.000 title description 15
- 230000006872 improvement Effects 0.000 title description 4
- 239000000126 substance Substances 0.000 title description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 25
- 239000000243 solution Substances 0.000 description 21
- 239000002253 acid Substances 0.000 description 20
- 239000000463 material Substances 0.000 description 20
- 238000004043 dyeing Methods 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000009835 boiling Methods 0.000 description 13
- 229920002994 synthetic fiber Polymers 0.000 description 10
- 238000011282 treatment Methods 0.000 description 10
- 229910052804 chromium Inorganic materials 0.000 description 9
- 239000011651 chromium Substances 0.000 description 9
- 239000000975 dye Substances 0.000 description 9
- 239000005018 casein Substances 0.000 description 8
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 8
- 235000021240 caseins Nutrition 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- 150000001845 chromium compounds Chemical class 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 6
- 238000007792 addition Methods 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 150000001844 chromium Chemical class 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- -1 chrome compound Chemical class 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 210000002268 wool Anatomy 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- BNQYBOIDDNFHHC-UHFFFAOYSA-N chromium;oxalic acid Chemical compound [Cr].OC(=O)C(O)=O BNQYBOIDDNFHHC-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000001117 sulphuric acid Substances 0.000 description 2
- 235000011149 sulphuric acid Nutrition 0.000 description 2
- AWFYPPSBLUWMFQ-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(1,4,6,7-tetrahydropyrazolo[4,3-c]pyridin-5-yl)ethanone Chemical group C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=C2 AWFYPPSBLUWMFQ-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229910021555 Chromium Chloride Inorganic materials 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 239000001828 Gelatine Substances 0.000 description 1
- 102000011782 Keratins Human genes 0.000 description 1
- 108010076876 Keratins Proteins 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 235000009470 Theobroma cacao Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000012237 artificial material Substances 0.000 description 1
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 1
- 244000240602 cacao Species 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910021563 chromium fluoride Inorganic materials 0.000 description 1
- QSWDMMVNRMROPK-UHFFFAOYSA-K chromium(3+) trichloride Chemical compound [Cl-].[Cl-].[Cl-].[Cr+3] QSWDMMVNRMROPK-UHFFFAOYSA-K 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- FTBATIJJKIIOTP-UHFFFAOYSA-K trifluorochromium Chemical compound F[Cr](F)F FTBATIJJKIIOTP-UHFFFAOYSA-K 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/046—Material containing basic nitrogen containing amide groups using metallisable or mordant dyes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L89/00—Compositions of proteins; Compositions of derivatives thereof
- C08L89/005—Casein
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F4/00—Monocomponent artificial filaments or the like of proteins; Manufacture thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/07—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof
- D06M11/11—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof with halogen acids or salts thereof
- D06M11/24—Halides of elements of Groups 6 or 16 of the Periodic Table, e.g. chromyl chloride
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/32—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond
- D06M11/36—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with oxygen, ozone, ozonides, oxides, hydroxides or percompounds; Salts derived from anions with an amphoteric element-oxygen bond with oxides, hydroxides or mixed oxides; with salts derived from anions with an amphoteric element-oxygen bond
- D06M11/48—Oxides or hydroxides of chromium, molybdenum or tungsten; Chromates; Dichromates; Molybdates; Tungstates
Definitions
- the present invention relates to a process for improving the dynamometric resistance and the stability to heat, to boiling water, to dyeing and other treatments of artificial masses and fibers prepared from protein-like substances.
- the present invention is an improvement and development of the invention described in the copending application Ser. No. 303,158 filed at the same date as the present patent application by Giampiero Comolli, and also assigned to the,
- Appropriate dyestufis are, besides the substantive and the sulphur dyestufis, acid and chrome dyestufis, which require; in order to be fixed on the fiber, the dyeing at the boiling temperature in presence of acid.
- the dyeings obtained on Lanital treated according to the present invention possess a much better looking and a smoother touch. They'also possess better fastness properties than on untreated Lanital insofar, as they withstand a washing with soap'and soda at 60 C. and even the milling, if the dyeing has been carried out with chrome dyestufis.-
- a further important improvement resides in that the treated fibers possess in wet and in dry" form a much higher mechanical resistance and elasticity in comparison with the untreated fibers.
- the treated fibers possess also a better resistance to wear and withstand the milling much better than untreated Lanital.
- the rapidity of the taking up of the chromium derivative depends on the sort of the chromium-compound and the temperature at which the operation is carried out. By suitable additions the operation can be made more rapid or slower; generally an addition of acid makes it more rapid, whereas the addition of salts or the use of basic chromium compounds makes it slower.
- the process is not limited to the use of aqueous baths, as the water can be replaced completely or partially by other solvents which do not dissolve the artificial material.
- the chromium compounds In order to obtain a good result it is preferable to use the chromium compounds in concentratedsolution and in an excess. One must not, thereforaas in themordanting of woolrwith chromium compounds, use only a small percentage thereof caiculated on the weight of material to be treated. It is necessary to use from the beginning great quantities of the chrome compounds.- The time of the treatment varies in wide limits and can be seen from the following examples; it is dependent from the sort of the, material to be treated, from its form, from temperature and from the reactivity of the selected chrome compound. After the treatment,
- the chrome compound which has not been utilized is separated from the material in any suitable way, for instance by pressing out, hydroextracting etc., and the treatedmaterial is carefully washed out with water.
- the regenerated solutions of the chromium salts can, after standardisation be used for the treatment of new lots of material.v
- the tanned wet material does not change on storing in wet form. If one will dye it with such dyestuffs that use acid for the dyeing, it can be dyed directly. If it is intended to dye it in a neutral or alkaline bath, it is preferable to treat the tanned material with acid binding agents like soda or ammonia in order to neutralize the small quantities of acids contained therein.
- the present tanning process can also be carried out during the manufacture of the artificial products.
- the tanning operation simultaneously with the dyeing of the fibers, for instance, when the artificial fibers are intended to be dyed with mordant dyestuffs in presence of salts of trivalent chromium and in one bath.
- the quantity of the chromium salt must be strongly increased in order that the artificial fiber becomes tanned and the chromium lake of the dyestufi becomes aproduced.
- Example 1 10 parts of the artificial fiber known under the trade name Lanital are treated during 5 minutes at 60 C. with a solution of parts of chrome alum in 100 parts of water, hydroextracted, then washed with cold water, treated during 1 minute with per cent ammonia solution, washed again, hydroextracted and dried.
- the Lanital treated in this manner is colored in a clear green, possesses a high lustre and a smooth touch. By dyeing in a boiling bath in presence oi sulphuric acid, the breakage resistance of the fiber is only slightly decreased and is much better than the resistance of the nontanned Lanital treated with the same acid bath.
- Example 2 Lanital yarn is treated during 30 minutes at boiling temperature in an aqueous 10 per cent chrome alum solution in a bath ratio 1:10, hydroextracted, well washed with cold water, then with water containing ammonia, then with fresh water and dried.
- the touch of the greenish dyed Lanital is smooth and its resistance against hot diluted acids and alkaliesis excellent.
- the above cited properties remain unaltered when the material is subjected to a dyeing operation.
- the tanned green Lanital is fast to storing i wet and dry condition.
- the tanning is carried out with the above said chrome alum solution under addition of 2% of sulphuric acid, calculated on the weight of the dry Lanital, the tanning is finished already after 10 minutes. After hydroextracting and washing, it is absolutely necessary to treat itin a bath containing an acid binding agent in order to neutralize the acid remaining in the fiber and which otherwise would destroy the material on drying.
- Example 3 Lanital yarn, is treated with 35% of chrome alum, calculated on the weight of the dry Lanital, in an aqueous bath during 30 minutes at C., whereby the Lanital becomes colored in a green shade. After the bath has been practically exhausted, the fiber is taken out, the bath is cooled down to 50 C. and to the bath is added the desired quantity of a mordant dyestuff and of Glauber salt and the necessary quantity of an acid and the tanned Lanital fiber is again immersed therein. The dyeing is then carried out in the usual manner and after chromed under addition of potassium bichromate at the boiling temperature. A dyed fiber possessing smooth touch, high elasticity and resistance to breakwill be obtained.
- Example 4 A mixed material consisting of equal parts of wool and of Lanital are treated during 30 minutes in a solution containing 50 grams of chrome alum per litre of water, whereby the treatment is carried out at the boil. After this time the mixed material is hydroextracted, washed with cold water, treated during 1 minute with a solution of ammonia of 0.25 per cent, washed again, hydroextracted and dried. By this tanning operation the properties of the Lanital become so far improved, that it withstands, without decrease of its properties, the long boiling necessary for the dyeing of the mixed material.
- Example 5 Lanital yarn is treated during 5 minutes at the boiling temperature with a 9 per cent aqueous solution of chrome chloride in a bath ratio 1:10, whereby a rapid and level wetting-out of the fiber takes place. The fibers are then hydroextracted, well washed with cold water, neutralized with water containing sodium carbonate, washed again, hydroextracted and dried.
- Example 6 10 parts of Lanital yarn are boiled during3 minutes in parts of a 10 per cent aqueous chrome fluoride solution, washed, neutralized and washed again.
- the yarn treated in this manner can be dyed with acid dyestuifs in presence of an acid at the boiling temperature without its fastness to breaking and its elasticitybeing decreased.
- the dyed yarn possesses the same fastness to washing as the respective dyeing on wool.
- Example 7 Lanital yarn is treated at'the boiling temperature and in a bath ratio 1:10 during 15 minutes in a 30% aqueous solution of chrome acetate to which have been added 1-2 grams of a, wetting agent consisting of cocoa fat acid polyglycerides per liter bath. After this treatment the yarn is hydroextracted, washed out and dried.
- a, wetting agent consisting of cocoa fat acid polyglycerides per liter bath.
- Example 8 Lanital in loose form is treated during 10 minutes with a boiling 30 per cent aqueous solution of complex sodium chrome oxalate. If it is intended to dye the material tanned in this manner with a mordant dyestuif such as Indochro mine 2R (Colour Index No, 931), it is not necessary to completely wash out the chrome solution, but the material is only hydroextracted and introduced into a die bath containing the dyestuff and the necessary quantity of the chrome mordant and acid. The dyeing is carried out in the usual manner.
- a mordant dyestuif such as Indochro mine 2R (Colour Index No, 931) it is not necessary to completely wash out the chrome solution, but the material is only hydroextracted and introduced into a die bath containing the dyestuff and the necessary quantity of the chrome mordant and acid. The dyeing is carried out in the usual manner.
- Example 9 The tanning operation can sometimes be carried out simultaneously with the dyeing. This is possible in the case where the used dyestufis are not precipitated by the chrome salts or altered in their shade: what happens in the case of many acid dyestuffs, or when mordant dyestuffs, which are developed by the treatment with trivalent chrome compounds, such as Indochromine 2R, are used.
- tanning as employed in the present specification is not intended to refer to tanning in the sense of converting untanned material into tanned material, but is rather intended to describe what may be termed a mordanting process, i. e. a process analogous to the mordanting of wool in order to prepare 'it for dyeing with chrome colors.
- a process for improving water-insoluble, ar-, tificial fibers prepared from solutions of casein comprising the step of treating the said fibers with a solution of a salt of trivalent chromium fibers, and subjecting the same to a treatment with an acid binding agent.
- a process for improving water-insoluble, artificial fibers prepared from solutions of casein comprising the steps of treating the said fibers with a solution of a salt of trivalent chromium at a temperature of at least 0., thereby causin the formation and fixation of a water-insoluble chromium compound in and on the treated fibers, and dyeing the treated fibers with a mordant dyestuff, without eliminating the excess of the chromium salt and of the acid formed.
- a process for improving water-insoluble, artificial fibers prepared from solutions of casein comprising the step of treating the said fibers in presence of a suitable dyestuff with a solution of a salt of trivalent chromium at a temperature of at least 50 C., thereby causing the formation and fixation of a water-insoluble chromium compound in and on the treated fibers.
- a process for improving water-insoluble, artificial fibers prepared from solutions of casein comprising, the step of treating the said fibers with an aqueou solution of chrome alum at a temperature of 50-100 C.
- a process for improving Water-insoluble, artificial fibers prepared from solutions of casein comprising the step of treating the said fibers with an aqueous solution of chromium fluoride at a temperature of 50-100 C.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Artificial Filaments (AREA)
Description
Patented Feb. 6, 1945 PROCESS FOR THE IIHPROVEMENT OF THE PROPERTIES OF ARTIFICIAL MASSES AND FIBERS MANUFACT LIKE SUBSTANCES URED FROM PROTEIN Walter Friedrich Tschudin, Basel, Switzerland,
assignor to firm of Sandoz A. G., Basel, Switzerland 7 No Drawing. Application November 6, 1939, Se-
iiglgNo. 303,128. In Switzerland January 27, 3
7 Claims.
The present invention relates to a process for improving the dynamometric resistance and the stability to heat, to boiling water, to dyeing and other treatments of artificial masses and fibers prepared from protein-like substances.
The present invention is an improvement and development of the invention described in the copending application Ser. No. 303,158 filed at the same date as the present patent application by Giampiero Comolli, and also assigned to the,
firm of Sandoz A. G.
It has been found that artificial masses and artificial fibers which have been prepared from albuminic or proteinic substances, like albumin, casein, gelatine, keratin, glue and the like, can be greatly improved in their properties when they are subjected to a tanning operation at a temperature above 50 C. with compounds of trivalent chromium, and eventually to a subsequent treatment with acid binding agents.
By the above treatment the formation and the fixation of water insoluble chrome compounds takes place in and on the treated material, whereoy its resistance towards boiling water, even in presence of organic and inorganic acids, is greatly improved. This improvement is especially re markable in the case of artificial fibers prepared from casein and known for instance under the trade-mark Lanital. Lanital, which has been tanned with chrome compounds according to the present process, can be dyed by the usual dyeing processes without decreasing the dynamometric resistance and other properties of the material.
Appropriate dyestufis are, besides the substantive and the sulphur dyestufis, acid and chrome dyestufis, which require; in order to be fixed on the fiber, the dyeing at the boiling temperature in presence of acid. The dyeings obtained on Lanital treated according to the present invention possess a much better looking and a smoother touch. They'also possess better fastness properties than on untreated Lanital insofar, as they withstand a washing with soap'and soda at 60 C. and even the milling, if the dyeing has been carried out with chrome dyestufis.-
A further important improvement resides in that the treated fibers possess in wet and in dry" form a much higher mechanical resistance and elasticity in comparison with the untreated fibers. The treated fibers possess also a better resistance to wear and withstand the milling much better than untreated Lanital.
For carrying out the present invention all compounds of trivalent chromium can be used,
but it is preferable to use such derivatives that are rapidly taken up. by the fiber. The rapidity of the taking up of the chromium derivative depends on the sort of the chromium-compound and the temperature at which the operation is carried out. By suitable additions the operation can be made more rapid or slower; generally an addition of acid makes it more rapid, whereas the addition of salts or the use of basic chromium compounds makes it slower. v
It is natural that the action of the tanning is the best, when the same. has been carried out levelly; therefore it is necessary to soak. the.
material in the solution. of the chrome compound as well as possible. For this purpose several mechanical means can be used. Sometimes it is also preferable to add wetting and penetrating agents that are active inthe presence of chromium compounds.
For carrying out the present process salts of the trivalent chromium with in-organic or organic acids and also double salts and complex salts like chrome chloride, chrome fiuoride,;
generally carried out in an aqueous medium,
whereby water soluble chromium salts are used.
But the process is not limited to the use of aqueous baths, as the water can be replaced completely or partially by other solvents which do not dissolve the artificial material.
In order to obtain a good result it is preferable to use the chromium compounds in concentratedsolution and in an excess. One must not, thereforaas in themordanting of woolrwith chromium compounds, use only a small percentage thereof caiculated on the weight of material to be treated. It is necessary to use from the beginning great quantities of the chrome compounds.- The time of the treatment varies in wide limits and can be seen from the following examples; it is dependent from the sort of the, material to be treated, from its form, from temperature and from the reactivity of the selected chrome compound. After the treatment,
the chrome compound which has not been utilized is separated from the material in any suitable way, for instance by pressing out, hydroextracting etc., and the treatedmaterial is carefully washed out with water. The regenerated solutions of the chromium salts can, after standardisation be used for the treatment of new lots of material.v
The tanned wet material does not change on storing in wet form. If one will dye it with such dyestuffs that use acid for the dyeing, it can be dyed directly. If it is intended to dye it in a neutral or alkaline bath, it is preferable to treat the tanned material with acid binding agents like soda or ammonia in order to neutralize the small quantities of acids contained therein.
In a similar way as with manufactured masses and fibers the present tanning process can also be carried out during the manufacture of the artificial products.- v
In some cases it is possible to carry out the tanning operation simultaneously with the dyeing of the fibers, for instance, when the artificial fibers are intended to be dyed with mordant dyestuffs in presence of salts of trivalent chromium and in one bath. In this case the quantity of the chromium salt must be strongly increased in order that the artificial fiber becomes tanned and the chromium lake of the dyestufi becomes aproduced.
The following examples, without being limitative, show how the present invention can be carried out.
Example 1 10 parts of the artificial fiber known under the trade name Lanital are treated during 5 minutes at 60 C. with a solution of parts of chrome alum in 100 parts of water, hydroextracted, then washed with cold water, treated during 1 minute with per cent ammonia solution, washed again, hydroextracted and dried. The Lanital treated in this manner is colored in a clear green, possesses a high lustre and a smooth touch. By dyeing in a boiling bath in presence oi sulphuric acid, the breakage resistance of the fiber is only slightly decreased and is much better than the resistance of the nontanned Lanital treated with the same acid bath.
Example 2 Lanital yarn is treated during 30 minutes at boiling temperature in an aqueous 10 per cent chrome alum solution in a bath ratio 1:10, hydroextracted, well washed with cold water, then with water containing ammonia, then with fresh water and dried. The touch of the greenish dyed Lanital is smooth and its resistance against hot diluted acids and alkaliesis excellent. The above cited properties remain unaltered when the material is subjected to a dyeing operation. The tanned green Lanital is fast to storing i wet and dry condition.
If the tanning is carried out with the above said chrome alum solution under addition of 2% of sulphuric acid, calculated on the weight of the dry Lanital, the tanning is finished already after 10 minutes. After hydroextracting and washing, it is absolutely necessary to treat itin a bath containing an acid binding agent in order to neutralize the acid remaining in the fiber and which otherwise would destroy the material on drying.
Example 3 Lanital yarn, is treated with 35% of chrome alum, calculated on the weight of the dry Lanital, in an aqueous bath during 30 minutes at C., whereby the Lanital becomes colored in a green shade. After the bath has been practically exhausted, the fiber is taken out, the bath is cooled down to 50 C. and to the bath is added the desired quantity of a mordant dyestuff and of Glauber salt and the necessary quantity of an acid and the tanned Lanital fiber is again immersed therein. The dyeing is then carried out in the usual manner and after chromed under addition of potassium bichromate at the boiling temperature. A dyed fiber possessing smooth touch, high elasticity and resistance to breakwill be obtained.
Example 4 A mixed material consisting of equal parts of wool and of Lanital are treated during 30 minutes in a solution containing 50 grams of chrome alum per litre of water, whereby the treatment is carried out at the boil. After this time the mixed material is hydroextracted, washed with cold water, treated during 1 minute with a solution of ammonia of 0.25 per cent, washed again, hydroextracted and dried. By this tanning operation the properties of the Lanital become so far improved, that it withstands, without decrease of its properties, the long boiling necessary for the dyeing of the mixed material.
Example 5 Lanital yarn is treated during 5 minutes at the boiling temperature with a 9 per cent aqueous solution of chrome chloride in a bath ratio 1:10, whereby a rapid and level wetting-out of the fiber takes place. The fibers are then hydroextracted, well washed with cold water, neutralized with water containing sodium carbonate, washed again, hydroextracted and dried.
If one will dye the material treated in this manner immediately after the tanning, it is no more necessary to neutralize and to dry the yarn, especially in the case where it is intended to dye the material in an acid bath.
Example 6 10 parts of Lanital yarn are boiled during3 minutes in parts of a 10 per cent aqueous chrome fluoride solution, washed, neutralized and washed again. The yarn treated in this manner can be dyed with acid dyestuifs in presence of an acid at the boiling temperature without its fastness to breaking and its elasticitybeing decreased. The dyed yarn possesses the same fastness to washing as the respective dyeing on wool.
Example 7 Lanital yarn is treated at'the boiling temperature and in a bath ratio 1:10 during 15 minutes in a 30% aqueous solution of chrome acetate to which have been added 1-2 grams of a, wetting agent consisting of cocoa fat acid polyglycerides per liter bath. After this treatment the yarn is hydroextracted, washed out and dried.
Example 8 Lanital in loose form is treated during 10 minutes with a boiling 30 per cent aqueous solution of complex sodium chrome oxalate. If it is intended to dye the material tanned in this manner with a mordant dyestuif such as Indochro mine 2R (Colour Index No, 931), it is not necessary to completely wash out the chrome solution, but the material is only hydroextracted and introduced into a die bath containing the dyestuff and the necessary quantity of the chrome mordant and acid. The dyeing is carried out in the usual manner.
Example 9 The tanning operation can sometimes be carried out simultaneously with the dyeing. This is possible in the case where the used dyestufis are not precipitated by the chrome salts or altered in their shade: what happens in the case of many acid dyestuffs, or when mordant dyestuffs, which are developed by the treatment with trivalent chrome compounds, such as Indochromine 2R, are used.
In this latter case one will Work as follows: To 300 parts of a 2 per cent sodium chromoxalate solution there is added the desired quantityv of the Indochromine 2R-solution and the necessary quantity of acetic or formic acid. 10 parts of Lanital yarn are then introduced into this bath, which is heated up to the boiling point hour, and boiled therein during 1 /2 hours. A yarn dyed of a blue shade will be obtained which, in spite of the long boiling period, possesses a much better touch and breakage fastness than a Lanital fiber which has been dyed in the same manner, but only in presence of the quantity of sodium chromoxalate which is necessary for forming the chromium lake of the dyestuif I'ndochromine 2R.
The term tanning as employed in the present specification is not intended to refer to tanning in the sense of converting untanned material into tanned material, but is rather intended to describe what may be termed a mordanting process, i. e. a process analogous to the mordanting of wool in order to prepare 'it for dyeing with chrome colors.
What I claim is:
1. A process for improving water-insoluble, ar-, tificial fibers prepared from solutions of casein, comprising the step of treating the said fibers with a solution of a salt of trivalent chromium fibers, and subjecting the same to a treatment with an acid binding agent.
3. A process for improving water-insoluble, artificial fibers prepared from solutions of casein, comprising the steps of treating the said fibers with a solution of a salt of trivalent chromium at a temperature of at least 0., thereby causin the formation and fixation of a water-insoluble chromium compound in and on the treated fibers, and dyeing the treated fibers with a mordant dyestuff, without eliminating the excess of the chromium salt and of the acid formed.
4. A process for improving water-insoluble, artificial fibers prepared from solutions of casein, comprising the step of treating the said fibers in presence of a suitable dyestuff with a solution of a salt of trivalent chromium at a temperature of at least 50 C., thereby causing the formation and fixation of a water-insoluble chromium compound in and on the treated fibers.
5. A process for improving water-insoluble, artificial fibers prepared from solutions of casein, comprising, the step of treating the said fibers with an aqueou solution of chrome alum at a temperature of 50-100 C.
6. A process for improving water-insoluble, artificial fibers prepared from-solutions of casein,
comprising the step of treating the said fibers with an aqueous solution of chromium chloride at a temperature of 50-100 C.
7. A process for improving Water-insoluble, artificial fibers prepared from solutions of casein, comprising the step of treating the said fibers with an aqueous solution of chromium fluoride at a temperature of 50-100 C.
WALTER .FRIEDRICH TSCHUDIN.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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IT536088X | 1938-11-14 | ||
CH536104X | 1939-01-27 |
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Publication Number | Publication Date |
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US2368690A true US2368690A (en) | 1945-02-06 |
Family
ID=25737527
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US303128A Expired - Lifetime US2368690A (en) | 1938-11-14 | 1939-11-06 | Process for the improvement of the properties of artificial masses and fibers manufactured from proteinlike substances |
US303158A Expired - Lifetime US2426861A (en) | 1938-11-14 | 1939-11-06 | Process for improving the properties of water-insoluble artificial protein fibres |
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Application Number | Title | Priority Date | Filing Date |
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US303158A Expired - Lifetime US2426861A (en) | 1938-11-14 | 1939-11-06 | Process for improving the properties of water-insoluble artificial protein fibres |
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US (2) | US2368690A (en) |
BE (1) | BE434686A (en) |
FR (1) | FR855286A (en) |
GB (2) | GB536088A (en) |
NL (1) | NL60511C (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2533356A (en) * | 1948-02-06 | 1950-12-12 | Borden Co | Casein filaments treated with mercuric salt and formaldehyde solution |
US2808346A (en) * | 1954-05-24 | 1957-10-01 | American Enka Corp | Method of treating an article of polymer containing polypeptide groups to render it unmeltable |
US3314743A (en) * | 1963-11-07 | 1967-04-18 | Gagliardi Domenick Donald | Processes for treatment of preformed articles of olefin polymers and resulting products |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2926061A (en) * | 1957-04-23 | 1960-02-23 | Varsenig Z Pasternak | Method of increasing the curl, filling power, etc., of land fowl feathers with zirconium sulfate and product produced thereby |
US2928713A (en) * | 1957-04-23 | 1960-03-15 | Varsenig Z Pasternak | Chromic acid treatment of feathers |
US3098696A (en) * | 1959-08-18 | 1963-07-23 | American Cyanamid Co | Manufacture of sterile surgical suture collagen |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US625345A (en) * | 1899-05-23 | Adam millar | ||
US77990A (en) * | 1868-05-19 | Improved mode of treating leather, cloth, and the like | ||
US836788A (en) * | 1905-07-17 | 1906-11-27 | Friedrich Todtenhaupt | Production of artificial silk and artificial hair from casein. |
FR356404A (en) * | 1905-07-25 | 1905-11-29 | Friedrich Todtenhaupt | Manufacturing process of artificial yarns for silks, horsehair and fabrics |
US950435A (en) * | 1908-12-22 | 1910-02-22 | Henri Louis Joseph Chavassieu | Process of obtaining proteo-cellulosic products. |
US1865497A (en) * | 1926-04-30 | 1932-07-05 | Technicolor | Method of hardening gelatine films and surfaces and resulting product |
US1968991A (en) * | 1933-01-30 | 1934-08-07 | Kraft Phenix Cheese Corp | Manufacture of transparent sheets or coatings |
NL42742C (en) * | 1934-09-19 | |||
US2046320A (en) * | 1934-10-25 | 1936-07-07 | Technicolor Motion Picture | Method of making hardened gelatin films and resulting product |
DE652322C (en) * | 1935-04-25 | 1937-10-28 | Freudenberg Carl Fa | Process for ironing tight stitches of fibers or threads from animal skin or tendon collagen |
BE417950A (en) * | 1935-10-22 | |||
NL46483C (en) * | 1937-05-11 | |||
US2140274A (en) * | 1937-08-12 | 1938-12-13 | Earle O Whittler | Fiber |
-
0
- NL NL60511D patent/NL60511C/xx active
- BE BE434686D patent/BE434686A/xx unknown
-
1939
- 1939-05-25 FR FR855286D patent/FR855286A/en not_active Expired
- 1939-07-27 GB GB21861/39A patent/GB536088A/en not_active Expired
- 1939-11-06 US US303128A patent/US2368690A/en not_active Expired - Lifetime
- 1939-11-06 US US303158A patent/US2426861A/en not_active Expired - Lifetime
- 1939-11-07 GB GB29562/39A patent/GB536104A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2533356A (en) * | 1948-02-06 | 1950-12-12 | Borden Co | Casein filaments treated with mercuric salt and formaldehyde solution |
US2808346A (en) * | 1954-05-24 | 1957-10-01 | American Enka Corp | Method of treating an article of polymer containing polypeptide groups to render it unmeltable |
US3314743A (en) * | 1963-11-07 | 1967-04-18 | Gagliardi Domenick Donald | Processes for treatment of preformed articles of olefin polymers and resulting products |
Also Published As
Publication number | Publication date |
---|---|
FR855286A (en) | 1940-05-07 |
US2426861A (en) | 1947-09-02 |
GB536104A (en) | 1941-05-02 |
BE434686A (en) | |
GB536088A (en) | 1941-05-02 |
NL60511C (en) |
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